Canonical Allele Identifier: CA381554015

Gene: AIP

Linked Data

• MyVariant Identifiers: chr11:g.67258049C>A (hg19) ; chr11:g.67490578C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490578C>A , CM000673.2:g.67490578C>A	GRCh38
NC_000011.9:g.67258049C>A , CM000673.1:g.67258049C>A	GRCh37
NC_000011.8:g.67014625C>A	NCBI36
NG_008969.1:g.12545C>A , LRG_460:g.12545C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.885C>A
ENST00000528641.7:c.598+121C>A	ENSP00000434982.3:n.598+121C>A
ENST00000529797.2:n.1420C>A
ENST00000682324.1:c.469-419C>A	ENSP00000508017.1:n.469-419C>A
ENST00000682659.1:c.418+121C>A	ENSP00000507351.1:n.418+121C>A
ENST00000682699.1:c.787+121C>A	ENSP00000507935.1:n.787+121C>A
ENST00000683237.1:c.779+129C>A	ENSP00000507343.1:n.779+129C>A
ENST00000683856.1:c.610+121C>A	ENSP00000507979.1:n.610+121C>A
ENST00000684006.1:c.787+121C>A	ENSP00000507269.1:n.787+121C>A
ENST00000684657.1:c.607+121C>A	ENSP00000507961.1:n.607+121C>A
ENST00000279146.8:c.787+121C>A MANE Select	ENSP00000279146.3:n.787+121C>A
ENST00000279146.7:c.787+121C>A	ENSP00000279146.3:n.787+121C>A
ENST00000525341.1:c.560C>A	ENSP00000476993.1:p.Pro187His
ENST00000528641.6:c.598+121C>A	ENSP00000434982.2:n.598+121C>A
NM_001302959.1:c.610+121C>A	NP_001289888.1:n.610+121C>A
NM_001302960.1:c.779+129C>A	NP_001289889.1:n.779+129C>A
NM_003977.3:c.787+121C>A	NP_003968.3:n.787+121C>A
XM_024448761.1:c.787+121C>A	XP_024304529.1:n.787+121C>A
NM_003977.4:c.787+121C>A MANE Select	NP_003968.3:n.787+121C>A
NM_001302960.2:c.779+129C>A	NP_001289889.1:n.779+129C>A
NM_001302959.2:c.610+121C>A	NP_001289888.1:n.610+121C>A